List of variants reported as uncertain significance for neurocristopathy by Equipe Genetique des Anomalies du Developpement, Université de Bourgogne

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro)	rs33927012	0.00921
NM_003000.3(SDHB):c.423+20T>A	rs190139590	0.00179
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.874G>A (p.Val292Met)	rs34682185	0.00023
NM_020975.6(RET):c.2556C>G (p.Ile852Met)	rs377767426	0.00011

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